Dilute solutions of glycogen from mussels (shellfish) and of different degradation steps were
investigated by static and dynamic light scattering, viscometry, and end group analysis of the reducing
end. The data were analyzed in comparison with theory for hyperbranched polymers. In the monomer of
the A
type, the functional group B2 (resulting in α(1, 6) linkages) has a much lower reactivity than
that of the B1 group (leading to α(1, 4) linkages and chain growth). Qualitative agreement in behavior
was found with the nonfractionated samples, but the effective branching density, derived from the applied
physical techniques, was found to be considerably lower than that known from chemical analysis. SEC
fractionation in on-line combination with multiple-angle laser light scattering and a viscosity detector
revealed molar mass distributions that are composed of two main components. These components differ
in their physical properties. The required examination was possible because R
g and [η] could be measured
for each slice. Shrinking factors g = R
g
2
b/R
g
2
lin and g‘ = [η]b/[η]lin were determined. The results of
quantitative analysis are discussed in relation to current theories.